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细胞连接是否参与卵黄蛋白原摄取的调控?基于 RNA 测序的鳗鲡研究的新见解

Are Cell Junctions Implicated in the Regulation of Vitellogenin Uptake? Insights from an RNAseq-Based Study in Eel, .

机构信息

Department of Zoology, University of Otago, 340 Great King Street, P.O. Box 56, Dunedin 9054, New Zealand.

出版信息

Cells. 2022 Feb 4;11(3):550. doi: 10.3390/cells11030550.

Abstract

At the onset of puberty, ovarian follicles become competent to incorporate large amounts of vitellogenin (Vtg). Using an RNAseq-based approach, transcriptomes from pre-vitellogenic (PV) and early vitellogenic (EV) ovaries from wild-caught eel, , were compared to investigate the expression of specific genes encoding cell junction proteins that could be involved in regulating Vtg uptake. Partial support was found for the mechanical barrier hypothesis proposing that the access of Vtg to the oolemma is restricted by a tight junction (TJ) network within the granulosa cell layer, which changes between the PV and EV stage. Among 25 genes encoding TJ-constituting proteins, five were down-regulated and two were up-regulated. A chemical barrier hypothesis stating that gap junctions (GJs) are involved in modulating Vtg uptake was not supported, as only five GJs were found to be expressed in the ovary with no significant changes in expression between stages. Furthermore, the endocytic pathway was found to be up-regulated during the PV-EV transition. Finally, the study showed that gene expression patterns may help identify suitable candidates involved in the regulation of Vtg uptake, and provided novel sequence data for , including putative Vtg receptors corresponding to Lr8 and Lrp13 members of the low-density lipoprotein receptor family.

摘要

在青春期开始时,卵巢滤泡变得能够摄取大量卵黄蛋白原 (Vtg)。本研究采用基于 RNAseq 的方法,比较了野生鳗鱼的预卵黄生成 (PV) 和早期卵黄生成 (EV) 卵巢的转录组,以研究可能参与调节 Vtg 摄取的特定编码细胞连接蛋白的基因表达。部分支持了机械屏障假说,该假说提出,Vtg 进入卵母细胞膜受颗粒细胞层内紧密连接 (TJ) 网络的限制,该网络在 PV 和 EV 阶段之间发生变化。在编码 TJ 组成蛋白的 25 个基因中,有 5 个下调,2 个上调。化学屏障假说认为间隙连接 (GJ) 参与调节 Vtg 摄取,但这一假说并未得到支持,因为仅发现 5 个 GJ 在卵巢中表达,在不同阶段之间表达没有明显变化。此外,在 PV-EV 转变过程中发现内吞途径被上调。最后,该研究表明基因表达模式有助于确定参与 Vtg 摄取调节的合适候选基因,并为 提供了新的序列数据,包括对应于低密度脂蛋白受体家族的 Lr8 和 Lrp13 成员的潜在 Vtg 受体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/8834532/d449001cdbcb/cells-11-00550-g001.jpg

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